Compliance Specialist

PQE Group; Cataluña; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

PQE Group is seeking an experienced Compliance Support Specialist for a project in Spain to drive GMP compliance for aseptic manufacturing and ensure quality documentation aligns with SOPs.

You will collaborate with QA, Manufacturing, Validation, Engineering, and Operations to ensure documentation accuracy and readiness for audits, inspections, and change controls. Fluent English and native Spanish are required.

Formación

• Experience in GMP-regulated pharmaceutical environments.
• Strong knowledge of sterile manufacturing and aseptic processing.
• Experience supporting compounding and filling operations, preferably using isolator technology.
• Familiarity with products presented in prefilled syringes.
• Good understanding of FDA regulations and EU GMP guidelines.
• Experience reviewing and updating SOPs, quality documentation, and quality system procedures.
• Native-level Spanish proficiency (mandatory).
• Fluent English.

Responsabilidades

• Provide GMP compliance and documentation support for the implementation of new aseptic manufacturing processes.
• Review, update, and align GMP documentation, SOPs, and work instructions with internal quality standards, FDA regulations, EU GMP requirements, and industry best practices.
• Perform documentation gap assessments and support remediation activities to ensure procedures are aligned with new process and operational requirements.
• Collaborate with QA, Manufacturing, Validation, Engineering, and Operations to ensure documentation accuracy, consistency, and compliance.
• Support document lifecycle management, including revision, approval, implementation, and archival.
• Provide compliance support for sterile manufacturing and aseptic processing activities, including compounding and isolator-based filling.
• Support audits and regulatory inspection readiness, as well as deviations, CAPAs, investigations, and change controls from a documentation and compliance perspective.
• Contribute to quality system improvements, risk assessments, and GMP compliance activities throughout the project lifecycle.

Conocimientos

GMP compliance experience

Sterile manufacturing knowledge

SOP review/update

Cross-functional collaboration

Documentation control

Herramientas

Isolator technology

Quality documentation systems

Descripción del empleo

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2,000 employees across Europe, Asia, and the Americas.

We are currently seeking an experienced Compliance Support Specialist for a project in Spain. The successful candidate will support compliance activities related to the implementation of a new aseptic manufacturing process, ensuring GMP compliance through the review, update, and harmonization of quality documentation and Standard Operating Procedures (SOPs).

Responsibilities include:

• Provide GMP compliance and documentation support for the implementation of new aseptic manufacturing processes.
• Review, update, and align GMP documentation, SOPs, and work instructions with internal quality standards, FDA regulations, EU GMP requirements, and industry best practices.
• Perform documentation gap assessments and support remediation activities to ensure procedures are aligned with new process and operational requirements.
• Collaborate with QA, Manufacturing, Validation, Engineering, and Operations to ensure documentation accuracy, consistency, and compliance.
• Support document lifecycle management, including revision, approval, implementation, and archival.
• Provide compliance support for sterile manufacturing and aseptic processing activities, including compounding and isolator-based filling.
• Support audits and regulatory inspection readiness, as well as deviations, CAPAs, investigations, and change controls from a documentation and compliance perspective.
• Contribute to quality system improvements, risk assessments, and GMP compliance activities throughout the project lifecycle.

Requirements:

• Experience working in GMP-regulated pharmaceutical environments.
• Strong knowledge of sterile manufacturing and aseptic processing.
• Previous experience supporting compounding and filling operations, preferably using isolator technology.
• Familiarity with products presented in prefilled syringes.
• Good understanding of FDA regulations and EU GMP guidelines.
• Experience reviewing and updating SOPs, quality documentation, and quality system procedures.
• Native-level Spanish proficiency (mandatory).
• Fluent English

Working at PQE Group

As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration, innovation, and professional growth. PQE Group offers the opportunity to work on international projects, develop specialized expertise, and collaborate with industry-leading pharmaceutical companies worldwide.